AlbaTraDIS: Comparative analysis of large datasets from parallel transposon mutagenesis experiments.


Journal

PLoS computational biology
ISSN: 1553-7358
Titre abrégé: PLoS Comput Biol
Pays: United States
ID NLM: 101238922

Informations de publication

Date de publication:
07 2020
Historique:
received: 09 05 2019
accepted: 23 05 2020
revised: 29 07 2020
pubmed: 18 7 2020
medline: 4 9 2020
entrez: 18 7 2020
Statut: epublish

Résumé

Bacteria need to survive in a wide range of environments. Currently, there is an incomplete understanding of the genetic basis for mechanisms underpinning survival in stressful conditions, such as the presence of anti-microbials. Transposon directed insertion-site sequencing (TraDIS) is a powerful tool to identify genes and networks which are involved in survival and fitness under a given condition by simultaneously assaying the fitness of millions of mutants, thereby relating genotype to phenotype and contributing to an understanding of bacterial cell biology. A recent refinement of this approach allows the roles of essential genes in conditional stress survival to be inferred by altering their expression. These advancements combined with the rapidly falling costs of sequencing now allows comparisons between multiple experiments to identify commonalities in stress responses to different conditions. This capacity however poses a new challenge for analysis of multiple data sets in conjunction. To address this analysis need, we have developed 'AlbaTraDIS'; a software application for rapid large-scale comparative analysis of TraDIS experiments that predicts the impact of transposon insertions on nearby genes. AlbaTraDIS can identify genes which are up or down regulated, or inactivated, between multiple conditions, producing a filtered list of genes for further experimental validation as well as several accompanying data visualisations. We demonstrate the utility of our new approach by applying it to identify genes used by Escherichia coli to survive in a wide range of different concentrations of the biocide Triclosan. AlbaTraDIS identified all well characterised Triclosan resistance genes, including the primary target, fabI. A number of new loci were also implicated in Triclosan resistance and the predicted phenotypes for a selection of these were validated experimentally with results being consistent with predictions. AlbaTraDIS provides a simple and rapid method to analyse multiple transposon mutagenesis data sets allowing this technology to be used at large scale. To our knowledge this is the only tool currently available that can perform these tasks. AlbaTraDIS is written in Python 3 and is available under the open source licence GNU GPL 3 from https://github.com/quadram-institute-bioscience/albatradis.

Identifiants

pubmed: 32678849
doi: 10.1371/journal.pcbi.1007980
pii: PCOMPBIOL-D-19-00740
pmc: PMC7390408
doi:

Substances chimiques

Anti-Infective Agents 0
DNA Transposable Elements 0
Triclosan 4NM5039Y5X

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1007980

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/CCG1860/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/R012504/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/F/000PR10349
Pays : United Kingdom

Déclaration de conflit d'intérêts

I have read the journal's policy and the authors of this manuscript have the following competing interests: AKT is a named inventor on patents utilising transposon mutagenesis and has a financial interest in a company commercialising the technology. IGC has financial interests in companies commercialising transposon mutagenesis.

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Auteurs

Andrew J Page (AJ)

Quadram Institute Bioscience, Norwich Research Park, Colney Lane, Norwich, United Kingdom.

Sarah Bastkowski (S)

Quadram Institute Bioscience, Norwich Research Park, Colney Lane, Norwich, United Kingdom.

Muhammad Yasir (M)

Quadram Institute Bioscience, Norwich Research Park, Colney Lane, Norwich, United Kingdom.

A Keith Turner (AK)

Quadram Institute Bioscience, Norwich Research Park, Colney Lane, Norwich, United Kingdom.

Thanh Le Viet (T)

Quadram Institute Bioscience, Norwich Research Park, Colney Lane, Norwich, United Kingdom.

George M Savva (GM)

Quadram Institute Bioscience, Norwich Research Park, Colney Lane, Norwich, United Kingdom.

Mark A Webber (MA)

Quadram Institute Bioscience, Norwich Research Park, Colney Lane, Norwich, United Kingdom.
University of East Anglia, Norwich Research Park, Norwich, United Kingdom.

Ian G Charles (IG)

Quadram Institute Bioscience, Norwich Research Park, Colney Lane, Norwich, United Kingdom.
University of East Anglia, Norwich Research Park, Norwich, United Kingdom.

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